Cleared Traditional

K051605 - SBI K-WIRES

K051605 is an FDA 510(k) clearance for SBI K-WIRES, manufactured by Small Bone Innovations, LLC. The device is a Class 2 Orthopedic device with product code HTY cleared through the Traditional 510(k) pathway after a 55-day FDA review.

K051605 · Small Bone Innovations, LLC · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2005
Decision
55d
Days
Class 2
Risk

K051605 is an FDA 510(k) clearance for the SBI K-WIRES. Classified as Pin, Fixation, Smooth (product code HTY), Class II - Special Controls.

Submitted by Small Bone Innovations, LLC (Morrisville, US). The FDA issued a Cleared decision on August 10, 2005 after a review of 55 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Small Bone Innovations, LLC devices

FDA 510(k) Submission Details - K051605

510(k) Number K051605 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 16, 2005
Decision Date August 10, 2005
Days to Decision 55 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
67d faster than avg
Panel avg: 122d · This submission: 55d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HTY Device Classification - Class 2, Special Controls

Product Code HTY Pin, Fixation, Smooth
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3040
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - HTY Pin, Fixation, Smooth

All 137
Devices cleared under the same product code (HTY) and FDA review panel - the closest regulatory comparables to K051605.
KMEDIC INTERNAL/EXTERNAL FIXATION DEVICES
K070561 · Teleflex Medical · May 2007
ARTHREX CROSSPIN, MODEL AR-1964P
K063719 · Arthrex, Inc. · Mar 2007
ARTHREX K-WIRE ,THREADED MODELS AR-8990 TO 899X, AR-8991T TO AR-899XT
K052736 · Arthrex, Inc. · Nov 2005
ARTHREX BIO-PIN
K050259 · Arthrex, Inc. · May 2005
MODIFICATION TO: INION OTPS BIODEGRADABLE PIN
K050275 · Inion , Ltd. · Mar 2005
PINN-ACL CROSSPIN
K043106 · Linvatec Corp. · Jan 2005